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Record W3151814574 · doi:10.1111/epi.16854

Diverse genetic causes of polymicrogyria with epilepsy

2021· article· en· W3151814574 on OpenAlexfundno aff

Bibliographic record

VenueEpilepsia · 2021
Typearticle
Languageen
FieldMedicine
TopicEpilepsy research and treatment
Canadian institutionsnot available
FundersWeill Institute for Neurosciences, University of California, San FranciscoNational Center for Advancing Translational SciencesNational Institute of Child Health and Human DevelopmentNational Institute of Allergy and Infectious DiseasesNational Human Genome Research InstituteNational Institute of Mental HealthNHLBI Division of Intramural ResearchNational Institute on AgingPatient-Centered Outcomes Research InstituteMedical Research CouncilEunice Kennedy Shriver National Institute of Child Health and Human DevelopmentUniversity of California, San FranciscoBill and Melinda Gates FoundationUniversity of WashingtonUniversità degli Studi di FirenzeUniversity of California, Los AngelesSchool of Medicine, Emory UniversityPerelman School of Medicine, University of PennsylvaniaSchool of Medicine, New York UniversityCenters for Disease Control and PreventionNational Institutes of HealthMonash UniversityPediatric Epilepsy Research FoundationEndocrine Fellows FoundationJ. Willard and Alice S. Marriott FoundationMultidisciplinary University Research InitiativeNational Institute of Neurological Disorders and StrokeZynerba PharmaceuticalsMcGill UniversityZogenixUniversity of North Carolina at Chapel HillSeqirusUCLA Health SystemEisaiCincinnati Children's Hospital Medical CenterIrving Medical Center, Columbia UniversityYale UniversityCure KidsEmory UniversityYork UniversityBiogenVanderbilt UniversityNational Institute of Diabetes and Digestive and Kidney DiseasesGilead SciencesHealth Research Council of New ZealandEpilepsiatutkimussäätiöVanderbilt University Medical CenterMuscular Dystrophy AssociationChildren's Hospital of PhiladelphiaAstraZenecaGW PharmaceuticalsUniversity of PennsylvaniaJohns Hopkins UniversityImperial College LondonNorthwell HealthEllison Medical FoundationNational Science Foundation
KeywordsPolymicrogyriaGeneticsBiologyEpilepsyExome sequencingGermlineMacrocephalyExomeCandidate geneCopy-number variationSingle-nucleotide polymorphismGeneHaploinsufficiencyPhenotypeGenomeGenotypeNeuroscience

Abstract

fetched live from OpenAlex

OBJECTIVE: We sought to identify novel genes and to establish the contribution of known genes in a large cohort of patients with nonsyndromic sporadic polymicrogyria and epilepsy. METHODS: We enrolled participants with polymicrogyria and their parents through the Epilepsy Phenome/Genome Project. We performed phenotyping and whole exome sequencing (WES), trio analysis, and gene-level collapsing analysis to identify de novo or inherited variants, including germline or mosaic (postzygotic) single nucleotide variants, small insertion-deletion (indel) variants, and copy number variants present in leukocyte-derived DNA. RESULTS: Across the cohort of 86 individuals with polymicrogyria and epilepsy, we identified seven with pathogenic or likely pathogenic variants in PIK3R2, including four germline and three mosaic variants. PIK3R2 was the only gene harboring more than expected de novo variants across the entire cohort, and likewise the only gene that passed the genome-wide threshold of significance in the gene-level rare variant collapsing analysis. Consistent with previous reports, the PIK3R2 phenotype consisted of bilateral polymicrogyria concentrated in the perisylvian region with macrocephaly. Beyond PIK3R2, we also identified one case each with likely causal de novo variants in CCND2 and DYNC1H1 and biallelic variants in WDR62, all genes previously associated with polymicrogyria. Candidate genetic explanations in this cohort included single nucleotide de novo variants in other epilepsy-associated and neurodevelopmental disease-associated genes (SCN2A in two individuals, GRIA3, CACNA1C) and a 597-kb deletion at 15q25, a neurodevelopmental disease susceptibility locus. SIGNIFICANCE: This study confirms germline and postzygotically acquired de novo variants in PIK3R2 as an important cause of bilateral perisylvian polymicrogyria, notably with macrocephaly. In total, trio-based WES identified a genetic diagnosis in 12% and a candidate diagnosis in 6% of our polymicrogyria cohort. Our results suggest possible roles for SCN2A, GRIA3, CACNA1C, and 15q25 deletion in polymicrogyria, each already associated with epilepsy or other neurodevelopmental conditions without brain malformations. The role of these genes in polymicrogyria will be further understood as more patients with polymicrogyria undergo genetic evaluation.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesInsufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.076
Threshold uncertainty score0.999

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.020
GPT teacher head0.285
Teacher spread0.265 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations30
Published2021
Admission routes1
Has abstractyes

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